Evidence map›Paper›PMID 31209217›Full record

ArticleScientific data2019

Multiplex RNA single molecule FISH of inducible mRNAs in single yeast cells.

Guoliang Li, Gregor Neuert

Abstract readDataset
In one paragraph

Article in Scientific data, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Computerized fluorescence microscopy of microbial cells.World journal of microbiology & biotechnology · 2021
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Guoliang LiDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN, 37232, USA.
Gregor NeuertDepartment of Molecular Physiology and Biophysics, School of Medicine, Vanderbilt University, Nashville, TN, 37232, USA. gregor.neuert@vanderbilt.edu.

Funding

DECODING THE NONCODING GENOME: LNCRNA DYNAMICS AND FUNCTION IN SINGLE CELLSDP2GM114849 · NIGMS · VANDERBILT UNIVERSITY · PI NEUERT, GREGOR · 2014 to 2014
$2.4M
Molecular Mechanism of Gene Transcription ActivationR01GM115892 · NIGMS · VANDERBILT UNIVERSITY · PI NEUERT, GREGOR · 2015 to 2018
$1.2M
High-Performance Computer Cluster for Biomedical ResearchS10OD023680 · OD · VANDERBILT UNIVERSITY · PI MEILER, JENS · 2017 to 2017
$587k
NIGMS NIH HHS DP2 GM114849NIGMS NIH HHS R01 GM115892NIH HHS S10 OD023680U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) DP2GM11484901U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) R01GM115892U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences (NIGMS) S10OD023680
6 · The paper itself

Abstract

Transcript levels powerfully influence cell behavior and phenotype and are carefully regulated at several steps. Recently developed single cell approaches such as RNA single molecule fluorescence in-situ hybridization (smFISH) have produced advances in our understanding of how these steps work within the cell. In comparison to single-cell sequencing, smFISH provides more accurate quantification of RNA levels. Additionally, transcript subcellular localization is directly visualized, enabling the analysis of transcription (initiation and elongation), RNA export and degradation. As part of our efforts to investigate how this type of analysis can generate improved models of gene expression, we used smFISH to quantify the kinetic expression of STL1 and CTT1 mRNAs in single Saccharomyces cerevisiae cells upon 0.2 and 0.4 M NaCl osmotic stress. In this Data Descriptor, we outline our procedure along with our data in the form of raw images and processed mRNA counts. We discuss how these data can be used to develop single cell modelling approaches, to study fundamental processes in transcription regulation and develop single cell image processing approaches.

Indexed as

In Situ Hybridization, FluorescenceRNA, FungalRNA, MessengerSingle-Cell AnalysisMembrane Transport ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsMembrane Transport ProteinsRNA, FungalRNA, MessengerSaccharomyces cerevisiae ProteinsSTL1 protein, S cerevisiae

Identifiers

PMID31209217
PMCPMC6572782

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.